Linked Data
gnomAD v4:
10-87709277-A-AG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87709281dup , CM000672.2:g.87709281dup | GRCh38 |
| NC_000010.10:g.89469038dup , CM000672.1:g.89469038dup | GRCh37 |
| NC_000010.9:g.89459018dup | NCBI36 |
| NG_012150.1:g.54563dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000456849.2:c.113dup MANE Select | ENSP00000406157.1:p.Gly39TrpfsTer? | |
| ENST00000361175.8:c.113dup | ENSP00000354436.4:p.Gly39TrpfsTer? | |
| ENST00000456849.1:c.113dup | ENSP00000406157.1:p.Gly39TrpfsTer? | |
| ENST00000465996.5:n.135dup | ||
| ENST00000482258.1:n.156dup | ||
| NM_001015880.1:c.113dup | NP_001015880.1:p.Gly39TrpfsTer? | |
| NM_004670.3:c.113dup | NP_004661.2:p.Gly39TrpfsTer? | |
| NM_001015880.2:c.113dup MANE Select | NP_001015880.1:p.Gly39TrpfsTer? | |
| NM_004670.4:c.113dup | NP_004661.2:p.Gly39TrpfsTer? |